| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58417495-58417550 | Rare:9 | ||||
| chr17:58487845-58488000 | Rare:37 | ||||
| chr17:58514527-58514736 | Rare:49 | ||||
| chr17:58517782-58517795 | Rare:3 | ||||
| chr17:58517804-58517934 | Common:1; Rare:27 | ||||
| chr17:58518263-58518584 | Rare:46 | ||||
| chr17:58692453-58692875 | Common:3; Rare:197; Clinvar:36; Clinvar (benign):34; Clinvar (pathogenic):3 | ||||
| chr17:59106274-59106485 | Common:1; Rare:61 | ||||
| chr17:59106653-59107284 | Common:5; Rare:193; Clinvar:6; Clinvar (benign):4 | ||||
| chr17:59154841-59155080 | Rare:71 | ||||
| chr17:59155136-59155502 | Common:2; Rare:84 | ||||
| chr17:59155555-59155835 | Rare:70 | ||||
| chr17:59209913-59210118 | Common:1; Rare:73 | ||||
| chr17:59220344-59220628 | Common:4; Rare:81 | ||||
| chr17:59565468-59565684 | Common:1; Rare:85 |